Evidence map›Paper›PMID 26566861›Full record

ArticleCell cycle (Georgetown, Tex.)2015

IL-12 induced the generation of IL-21- and IFN-γ-co-expressing poly-functional CD4+ T cells from human naive CD4+ T cells.

Sifei Yu, Lei Jia, Yannan Zhang, Junmin Zhong, Binyan Yang, Changyou Wu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 35 citations in OpenAlex.

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  10. Tissue-Resident Memory-Like CD8Journal of immunology research · 2021
    Observational
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  19. Immune Reconstitution Disorders: Spotlight on Interferons.International journal of biomedical investigation · 2019
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Sifei Yua Institute of Immunology; Zhongshan School of Medicine; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology; Sun Yat-sen University ; Guangzhou , China.
Lei Jiaa Institute of Immunology; Zhongshan School of Medicine; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology; Sun Yat-sen University ; Guangzhou , China.
Yannan Zhanga Institute of Immunology; Zhongshan School of Medicine; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology; Sun Yat-sen University ; Guangzhou , China.
Junmin Zhongb Guangzhou Women and Children's Medical Center ; Guangzhou , China.
Binyan Yanga Institute of Immunology; Zhongshan School of Medicine; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology; Sun Yat-sen University ; Guangzhou , China.
Changyou Wua Institute of Immunology; Zhongshan School of Medicine; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology; Sun Yat-sen University ; Guangzhou , China.
Institute of Immunology · HRGuangzhou Medical University · CNSun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukine-12 is critical for the differentiation of Th1 cells and can improve the development of Th1 cells with Tfh cell features in mouse model. Human effector CD4(+) T cells also exhibit poly-functionality by co-expressing IL-21 and IFN-γ. However, the effects of IL-12 on regulating generation of human IL-21- and IFN-γ-expressing CD4(+) T cells are still incompletely understood. Our studies found that IL-12 but not IL-21 could induce the differentiation of human naive CD4(+) T cells into multi-cytokine expressing CD4(+) T cells in vitro, which co-expressed IL-21 and IFN-γ with or without IL-2 and TNF-α. At early stage of differentiation, addition of excess exogenous IFN-γ could increase the generation of IL-21- and IFN-γ-expressing CD4(+) T cells, furthermore, anti-IFN-γ depressed the percentage of poly-functional CD4(+) T cells. Phenotypically, IL-21(+)IFN-γ(+)CD4(+) T cells exhibited more characteristic features about both of Th1 and Tfh cells than IL-21 or IFN-γ single-expressing CD4(+) T cells. Mechamistically, IL-12 modulated the differentiation of IL-21(+)IFN-γ(+)CD4(+) T cells from naive CD4(+) T cells via the pathways of STAT-1/4, T-bet and BCL(-)6. Different from naive CD4(+) T cells, IL-12 increasing the generation of IL-21(+)IFN-γ(+)CD4(+) T cells from memory CD4(+) T cells was only involved in STAT-4 pathway but not STAT-1. Poly-functional CD4(+) T cells were contributed to generation and progress of varies diseases and our studies provide basic theoretics for the designs of vaccine and therapies of diseases.

Indexed as

CD4-Positive T-LymphocytesCell DifferentiationCells, CulturedDNA-Binding ProteinsFetal BloodHumansImmunologic MemoryInfant, NewbornInterferon-gammaInterleukin-12Interleukin-21InterleukinsKineticsPhenotypeProto-Oncogene Proteins c-bcl-6Signal TransductionBCL6 protein, humanDNA-Binding ProteinsIFNG protein, humanInterferon-gammaInterleukin-12Interleukin-21InterleukinsProto-Oncogene Proteins c-bcl-6STAT1 protein, humanSTAT1 Transcription FactorSTAT4 protein, humanSTAT4 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsdifferentiationhumanIL-12IL-21poly-functional CD4+ T cells

Identifiers

PMID26566861
PMCPMC4825544
OpenAlexW2178251874

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.